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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 72149생성일: 2026년 10월 23일

Triethylamine → [(R)-3-((S)-2-benzyloxycarbonylamino-3-methyl-butyrylamino)-2-hydroxy-propyl]-cyclohexylmethyl-phosphinic acid benzyl ester

https://huagongshe.com/ko/reaction/72149

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물CarbodiimideHCID 160435—
반응물N-Carbobenzoxy-L-valineHCID 726987—
반응물((R)-3-amino-2-hydroxy-propyl)-cyclohexylmethyl-phosphinic acid benzyl ester hydrochlorideHCID 68622110—
반응물HCID 178418300HCID 178418300—
용매DichloromethaneHCID 6344—
생성물[(R)-3-((S)-2-benzyloxycarbonylamino-3-methyl-butyrylamino)-2-hydroxy-propyl]-cyclohexylmethyl-phosphinic acid benzyl esterHCID 6862094226.9%

반응 단계

To a solution of N-Cbz-L-valine (1.0 g, 3.98 mmol) dissolved in CH2Cl2 (80 mL) under nitrogen was added hydroxybenzotriazole (0.538 g, 3.98 mmol) and PS-Carbodiimide (2.25 g, 5.17 mmol). After stirring for 10 min, triethylamine (0.665 mL, 4.78 mmol) and ((R)-3-amino-2-hydroxy-propyl)-cyclohexylmethyl-phosphinic acid benzyl ester hydrochloride (1.44 g, 3.98 mmol) were added. The reaction was stirred for 2 h, then filtered and concentrated in vacuo. The residue was purified by flash chromatography with methanol/dichloromethane on a 35 g RediSep disposable column to give [(R)-3-((S)-2-benzyloxycarbonylamino-3-methyl-butyrylamino)-2-hydroxy-propyl]-cyclohexylmethyl-phosphinic acid benzyl ester (0.60 g, 1.07 mmol) as a white foam. NMR and MS spectra were substantially similar to the product obtained via Method A set forth above.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08828974B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-3566b976c00948f68d243c612bfd079f
출처 메모uspto-grants-2014_09